The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

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Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 10-25

Oxford University Press

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Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

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Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 467-476

Oxford University Press

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Analysis of Argonaute 4-Associated Long Non-Coding RNA in Arabidopsis thaliana Sheds Novel Insights into Gene Regulation through RNA-Directed DNA Methylation

By Au Phil Chi Khang   Dennis Elizabeth S.   Wang Ming-Bo  

Genes, Vol. 8, Iss. 8, 2017-08 ,pp. : 198-198

MDPI

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome

By Olney A.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1317-1325

Oxford University Press

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Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3

By Kim J.   Kollhoff A.   Bergmann A.   Stubbs L.  

Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 233-245

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